Assessing the Impact of Caring for a Person with Schizophrenia: Development of the Schizophrenia Caregiver Questionnaire

被引:18
作者
Gater, Adam [1 ]
Rofail, Diana [2 ]
Marshall, Chris [1 ]
Tolley, Chloe [1 ]
Abetz-Webb, Linda [1 ]
Zarit, Steven H. [3 ]
Berardo, Carmen Galani [4 ]
机构
[1] Adelphi Values Ltd, Bollington SK10 5JB, Cheshire, England
[2] Roche Prod Ltd, Welwyn Garden City AL7 3AY, Herts, England
[3] Penn State Univ, Coll Hlth & Human Dev, Dept Human Dev & Family Studies, University Pk, PA 16802 USA
[4] F Hoffmann La Roche & Co Ltd, CH-4002 Basel, Switzerland
关键词
QUALITY-OF-LIFE; FAMILY CAREGIVERS; ZARIT-BURDEN; SUBJECTIVE BURDEN; EXPRESSED EMOTION; COPING STRATEGIES; CONTENT VALIDITY; DATA SATURATION; SOCIAL SUPPORT; ADULT CHILDREN;
D O I
10.1007/s40271-015-0114-3
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
The responsibilities of caring for a person with schizophrenia may significantly impact informal caregivers' lives. The Zarit Burden Interview (ZBI) was originally developed to assess burden among caregivers of people with Alzheimer's disease. This research was conducted to inform the development of a revised version of the ZBI, relevant to caregivers of people with schizophrenia. Based on published qualitative research, the questionnaire was reviewed and modified in accordance with industry-standard guidelines. The resulting questionnaire [the Schizophrenia Caregiver Questionnaire (SCQ)] was then completed by 19 caregivers during cognitive debriefing interviews to assess understanding, relevance and comprehensiveness. Review of the ZBI resulted in a number of operational changes to improve face validity and potential sensitivity. Further questions were added based on key concepts identified in existing literature and minor phrasing alterations were made to improve content validity. Findings from caregiver interviews supported the content validity of the SCQ. The SCQ provides a comprehensive view of caregivers' subjective experiences of caregiving and demonstrated strong face and content validity. The questionnaire will be important in both clinical assessment and evaluating the efficacy of interventions designed to reduce or alleviate caregiver burden. Future research will seek to establish the psychometric validity of the questionnaire.
引用
收藏
页码:507 / 520
页数:14
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